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Dynamics of cancerous tissue correlates with invasiveness
Two of the classical hallmarks of cancer are uncontrolled cell division and tissue invasion, which turn the disease into a systemic, life-threatening condition. Although both processes are studied, a clear correlation between cell division and motility of cancer cells has not been described previous...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338316/ https://www.ncbi.nlm.nih.gov/pubmed/28262796 http://dx.doi.org/10.1038/srep43800 |
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author | West, Ann-Katrine Vransø Wullkopf, Lena Christensen, Amalie Leijnse, Natascha Tarp, Jens Magelund Mathiesen, Joachim Erler, Janine Terra Oddershede, Lene Broeng |
author_facet | West, Ann-Katrine Vransø Wullkopf, Lena Christensen, Amalie Leijnse, Natascha Tarp, Jens Magelund Mathiesen, Joachim Erler, Janine Terra Oddershede, Lene Broeng |
author_sort | West, Ann-Katrine Vransø |
collection | PubMed |
description | Two of the classical hallmarks of cancer are uncontrolled cell division and tissue invasion, which turn the disease into a systemic, life-threatening condition. Although both processes are studied, a clear correlation between cell division and motility of cancer cells has not been described previously. Here, we experimentally characterize the dynamics of invasive and non-invasive breast cancer tissues using human and murine model systems. The intrinsic tissue velocities, as well as the divergence and vorticity around a dividing cell correlate strongly with the invasive potential of the tissue, thus showing a distinct correlation between tissue dynamics and aggressiveness. We formulate a model which treats the tissue as a visco-elastic continuum. This model provides a valid reproduction of the cancerous tissue dynamics, thus, biological signaling is not needed to explain the observed tissue dynamics. The model returns the characteristic force exerted by an invading cell and reveals a strong correlation between force and invasiveness of breast cancer cells, thus pinpointing the importance of mechanics for cancer invasion. |
format | Online Article Text |
id | pubmed-5338316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53383162017-03-08 Dynamics of cancerous tissue correlates with invasiveness West, Ann-Katrine Vransø Wullkopf, Lena Christensen, Amalie Leijnse, Natascha Tarp, Jens Magelund Mathiesen, Joachim Erler, Janine Terra Oddershede, Lene Broeng Sci Rep Article Two of the classical hallmarks of cancer are uncontrolled cell division and tissue invasion, which turn the disease into a systemic, life-threatening condition. Although both processes are studied, a clear correlation between cell division and motility of cancer cells has not been described previously. Here, we experimentally characterize the dynamics of invasive and non-invasive breast cancer tissues using human and murine model systems. The intrinsic tissue velocities, as well as the divergence and vorticity around a dividing cell correlate strongly with the invasive potential of the tissue, thus showing a distinct correlation between tissue dynamics and aggressiveness. We formulate a model which treats the tissue as a visco-elastic continuum. This model provides a valid reproduction of the cancerous tissue dynamics, thus, biological signaling is not needed to explain the observed tissue dynamics. The model returns the characteristic force exerted by an invading cell and reveals a strong correlation between force and invasiveness of breast cancer cells, thus pinpointing the importance of mechanics for cancer invasion. Nature Publishing Group 2017-03-06 /pmc/articles/PMC5338316/ /pubmed/28262796 http://dx.doi.org/10.1038/srep43800 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article West, Ann-Katrine Vransø Wullkopf, Lena Christensen, Amalie Leijnse, Natascha Tarp, Jens Magelund Mathiesen, Joachim Erler, Janine Terra Oddershede, Lene Broeng Dynamics of cancerous tissue correlates with invasiveness |
title | Dynamics of cancerous tissue correlates with invasiveness |
title_full | Dynamics of cancerous tissue correlates with invasiveness |
title_fullStr | Dynamics of cancerous tissue correlates with invasiveness |
title_full_unstemmed | Dynamics of cancerous tissue correlates with invasiveness |
title_short | Dynamics of cancerous tissue correlates with invasiveness |
title_sort | dynamics of cancerous tissue correlates with invasiveness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5338316/ https://www.ncbi.nlm.nih.gov/pubmed/28262796 http://dx.doi.org/10.1038/srep43800 |
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